158468-93-0Relevant articles and documents
A facile one-pot sonochemical synthesis of surface-coated mannosyl protein microspheres for detection and killing of bacteria
Skirtenko, Natalia,Richman, Michal,Nitzan, Yeshayahu,Gedanken, Aharon,Rahimipour, Shai
, p. 12277 - 12279 (2011)
We report a remarkably facile one-pot sonochemical approach to prepare protein microspheres whose shells are covalently decorated with a mannosyl derivative to target Escherichia coli (E. coli), while their cores are encapsulated with tetracycline. Conjugated microspheres induced the agglutination of E. coli and increased the anti-bacterial activity of the encapsulated tetracycline by five fold.
Glucose- and pH-responsive controlled release of cargo from protein-gated carbohydrate-functionalized mesoporous silica nanocontainers
Wu, Shanshan,Huang, Xuan,Du, Xuezhong
supporting information, p. 5580 - 5584 (2013/06/27)
Learning to let go: Controlled release of cargo (purple cubes) from lectin (blue squares)-gated nanopores was achieved using mannose (green loops)-functionalized mesoporous silica (see scheme). The protein nanogates could be opened either by decreasing the pH of the buffer or by adding competing glucose (yellow rings) to release the cargo from the pores. Copyright
Synthesis of Clustered Glycoside - Antigen Conjugates by Two One-Pot, Orthogonal, Chemoselective Ligation Reactions: Scope and Limitations
Grandjean, Cyrille,Gras-Masse, Helene,Melnyk, Oleg
, p. 230 - 240 (2007/10/03)
Major histocompatibility class II antigens have been bound to clustered glycosides for selective targeting of the dendritic cell mannose receptor. Di-, tetra-, and octavalent glycoside - antigen conjugates have been obtained after two, orthogonal, hydrazo
